Anti-CXCL9 antibody [EPR23999-5] - BSA and Azide free (ab277639)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR23999-5] to CXCL9 - BSA and Azide free
- Suitable for: WB, IP, Flow Cyt
- Reacts with: Human
Overview
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Product name
Anti-CXCL9 antibody [EPR23999-5] - BSA and Azide free
See all CXCL9 primary antibodies -
Description
Rabbit monoclonal [EPR23999-5] to CXCL9 - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: WB, IP, Flow Cytmore details
Unsuitable for: ICC or IHC-P -
Species reactivity
Reacts with: Human -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: THP-1 (treated with 200ng/ml IFN-? and 50 ng/ml LPS(Lipopolysaccharide) for 24 hours) whole cell lysate; His-tagged human purified recombinant full-length protein CXCL9. Flow cyt: THP-1 (treated with 100ng/ml IFN-gamma and 1ug/ml LPS(Lipopolysaccharide) for 48 hours) cells. IP: THP-1 (treated with 100ng/ml IFN-gamma and 1ug/ml LPS(Lipopolysaccharide) for 48 hours) whole cell lysate.
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General notes
ab277639 is the carrier-free version of ab263442. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
ab277639 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. -
Storage buffer
Constituent: 100% PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR23999-5 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-CXCL9 antibody [EPR23999-5] (ab263442) at 1/1000 dilution
Lane 1 : Untreated THP-1 (human monocytic leukemia monocyte), whole cell lysate
Lane 2 : THP-1 treated with /ml IFN-gamma and 50 ng/ml LPS(Lipopolysaccharide) for 24 hours, whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/50000 dilution
Predicted band size: 14 kDa
Observed band size: 13,14 kDa why is the actual band size different from the predicted?This data was developed using ab263442, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The expression profile is consistent with what has been described in the literature (PMID: 15154616, 22973274).
Exposure time: 3 minutes.
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This data was developed using ab263442, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol-permeabilized THP-1 (human monocytic leukemia monocyte) treated with 100ng/ml IFN-γand 1ug/ml LPS (Lipopolysaccharide) for 48 hours (Red)/ Untreated control (Green) cells labelling CXCL9 with ab263442 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) isotype control (Black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
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This data was developed using ab263442, the same antibody clone in a different buffer formulation.
CXCL9 was immunoprecipitated from 0.35 mg THP-1(human monocytic leukemia monocyte) (treated with 100ng/ml IFN-γ and 1ug/ml LPS (Lipopolysaccharide) for 48 hours) whole cell lysate with ab263442 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab263442 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1: THP-1 treated with 100ng/ml IFN-γ and 1ug/ml LPS (Lipopolysaccharide) for 48 hours, whole cell lysate 10 ug
Lane 2: ab263442 IP in THP-1 treated with 100ng/ml IFN-γ and 1ug/ml LPS(Lipopolysaccharide) for 48 hours whole cell lysate
Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab263442 in THP-1 treated with 100ng/ml IFN-γ and 1ug/ml LPS(Lipopolysaccharide) for 48 hours whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 3 minutes.
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Anti-CXCL9 antibody [EPR23999-5] (ab263442) at 1/1000 dilution + His-tagged human purified recombinant full-length protein CXCL9, 10 ng
Secondary
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/50000 dilution
Predicted band size: 14 kDa
Observed band size: 13,14 kDa why is the actual band size different from the predicted?This data was developed using ab263442, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The expression profile is consistent with what has been described in the literature (PMID: 15154616, 22973274).
Exposure time: 5.5 seconds.
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